Electrolytic solution and battery

ABSTRACT

Provided is an electrolytic solution including a nonaqueous solvent and an alkali metal salt. The alkali metal salt is dissolved in the nonaqueous solvent. The nonaqueous solvent contains a perfluoropolyether and a fluorinated phosphate. Also provided is a battery including the electrolytic solution, a positive electrode containing a positive electrode active material that can occlude and release an alkali metal cation, and a negative electrode containing a negative electrode active material that can occlude and release the alkali metal cation.

BACKGROUND

1. Technical Field

The present disclosure relates to an electrolytic solution for batteriesand a battery including the electrolytic solution.

2. Description of the Related Art

Japanese Unexamined Patent Application Publication No. 2006-269374discloses a lithium ion battery including an electrolytic solutioncontaining a room temperature molten salt electrolyte comprising aperfluoropolyether.

In the electrolytic solution disclosed in Japanese Unexamined PatentApplication Publication No. 2006-269374, the perfluoropolyether is addedto the room temperature molten salt electrolyte in a proportion of 0.2%or more and 5% or less.

SUMMARY

One non-limiting and exemplary embodiment provides an electrolyticsolution having higher safety, which has been demanded in knowntechniques.

In one general aspect, the techniques disclosed here feature anelectrolytic solution containing a nonaqueous solvent and an alkalimetal salt. The alkali metal salt is dissolved in the nonaqueoussolvent. The nonaqueous solvent contains a perfluoropolyether and afluorinated phosphate. In one general aspect, the techniques disclosedhere feature a battery including the above-mentioned electrolyticsolution, a positive electrode containing a positive electrode activematerial that has a property of occluding and releasing an alkali metalcation, and a negative electrode containing a negative electrode activematerial that has a property of occluding and releasing the alkali metalcation.

The present disclosure can achieve an electrolytic solution having highsafety.

Additional benefits and advantages of the disclosed embodiments willbecome apparent from the specification and drawings. The benefits and/oradvantages may be individually obtained by the various embodiments andfeatures of the specification and drawings, which need not all beprovided in order to obtain one or more of such benefits and/oradvantages.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGURE is a schematic cross-sectional view illustrating an example ofthe battery according to Embodiment 2.

DETAILED DESCRIPTION

Embodiments of the present disclosure will now be described.

The viewpoints of the present inventor are described below.

Perfluoropolyethers and molecules having a perfluoropolyether skeletonhave low compatibility to nonaqueous electrolytic solutions. Therefore,the amount of a perfluoropolyether or a molecule having aperfluoropolyether skeleton that can be added to a nonaqueouselectrolytic solution is disadvantageously restricted to a narrow range.

For example, in Japanese Unexamined Patent Application Publication No.2006-269374, the amount of the perfluoropolyether is limited to 5% orless.

Thus, if a perfluoropolyether is added to a nonaqueous electrolyticsolution in an amount higher than a certain proportion (e.g., 5% ormore), the perfluoropolyether cannot be uniformly mixed with thenonaqueous electrolytic solution, and the performance as an electrolyticsolution cannot be shown.

On the basis of the above-mentioned viewpoints, the present inventor hasarrived at the creation of the composition of the present disclosure.

Embodiment 1

The electrolytic solution in Embodiment 1 contains a nonaqueous solventand an alkali metal salt.

The alkali metal salt is composed of an alkali metal cation and ananion.

The alkali metal salt is dissolved in the nonaqueous solvent.

The nonaqueous solvent contains a perfluoropolyether and a fluorinatedphosphate.

In the composition described above, the alkali metal salt issufficiently dissolved, and no phase separation occurs between theperfluoropolyether solvent and the fluorinated phosphate solvent as athird component. Accordingly, a perfluoropolyether can be mixed with anonaqueous solvent at an arbitrary ratio and at a higher ratio. That is,a large amount of a perfluoropolyether can be uniformly mixed with anonaqueous solvent. Consequently, for example, the electrolytic solutioncan have high flame retardancy, while keeping the function as anelectrolytic solution. Thus, a nonaqueous electrolytic solution havinghigher safety can be achieved.

The perfluoropolyether is a flame retardant solvent and has a lowpolarity caused by the smallness in the fluctuation of electrons due tothe large electronegativity of fluorine atoms. Consequently, theperfluoropolyether has low dissolving properties for salts and thereforecannot dissolve a large amount of a salt, unlike the solvents that areused in known nonaqueous electrolytic solutions.

The smallness of the polarity also causes low compatibility with usualorganic solvents having high polarity. In other words, the low polarityprevents the perfluoropolyether from penetrating between the moleculesof an organic solvent having a high polarity and large intermolecularforces. Consequently, the perfluoropolyether cannot be mixed with anorganic solvent.

That is, in the viewpoint of the internal energy of a material, theinternal energy form in the phase separated state is more stable thanthat in the uniformly compatibilized state.

As in stabilization of a polar organic solvent by the intermolecularforces derived from the polarity, the perfluoropolyether stabilizes theenergy through the high affinity between fluorine atoms orintermolecular forces increasing with the molecular chain length.

The perfluoropolyether contained in the nonaqueous electrolytic solutionof Embodiment 1 has a plurality of ether oxygen atoms in the moleculeand has fluorine atoms substituted for the hydrogen atoms on all alkylcarbon atoms. For example, the perfluoropolyether of Embodiment 1 may beCF₃—O—(CF₂—CF(CF₃)—O)_(p)—(CF₂—O)_(q)—CF₃ orCF₃—O—(C₃F₆—O)_(p)—(CF₂—O)_(q)—CF₃.

The nonaqueous electrolytic solution of Embodiment 1 is used in, forexample, a lithium secondary battery. Accordingly, the boiling point ofthe perfluoropolyether is preferably 60° C. or more, from the viewpointof the general operation temperature of lithium secondary batteries.That is, in order to achieve such a boiling point, theperfluoropolyether preferably has a weight-average molecular weight ofabout 350 or more.

An increase in the weight-average molecular weight causes an increase inthe viscosity. Accordingly, the weight-average molecular weight ispreferably also less than 1100.

The numbers, “p” and “q”, of the repeating units in the chemical formulaof the perfluoropolyether shown above are preferably selected such thatthe compound has a weight-average molecular weight of about 350 or moreand 1100 or less. The perfluoropolyether may be a block copolymer or arandom copolymer.

The perfluoropolyether may be a single compound or may be a compoundhaving two or more different substituents or may be a mixture ofstructural isomers having the same substituent.

Herein, the weight-average molecular weight (Mw) is determined bymultiplying the weight of each molecule by the molecular weight of themolecule, summing the resulting products, and dividing the resulting sumby the total weight.

Experimentally, the weight-average molecular weight can be determined bygel permeation chromatography (GPC) measurement. The GPC is one type ofliquid chromatography for performing separation based on the differencein molecular size and is a method for measuring the molecular weightdistribution and average molecular weight distribution of a highmolecular weight material. In addition, use of a light scatteringdetector in the GPC can provide absolute molecular weight distributionand weight-average molecular weight of a polymer material and alsoinformation, such as the radius of rotation.

The perfluoropolyether can be synthesized by a known reaction, such asphotooxidation of a perfluoroolefin or anionic polymerization of theepoxide of a perfluoroalkane. In the product synthesized by such areaction, the degree of polymerization (i.e., the molecular weight ofthe product) varies depending on the degree of the reaction progress. Adesired molecular weight of the product can be obtained by precisiondistillation or column purification.

In the electrolytic solution of Embodiment 1, the fluorinated phosphatemay contain a compound represented by Formula (1):

where, R₁ to R₃ each independently represent an aromatic group, anunsaturated aliphatic group, or a saturated aliphatic group.

The aromatic group, the unsaturated aliphatic group, and the saturatedaliphatic group may have at least one fluorine atom substituted for thehydrogen atom and may contain a halogen atom, a nitrogen atom, an oxygenatom, a sulfur atom, or a silicon atom.

The unsaturated aliphatic group and the saturated aliphatic group arestraight chains or are cyclic.

The composition described above can sufficiently dissolve an alkalimetal, has a high ionic conductivity, and also can provide anelectrolytic solution having excellent resistance to oxidation.Consequently, the composition can contribute to the charging anddischarging reaction of an active material that can provide a highvoltage of a 4-V level.

As described above, in Embodiment 1, a fluorinated phosphate, which isan aprotic solvent, can be used.

The phosphate solvent has a P═O double bond composed of a phosphorusatom P and an oxygen atom O and having a large bond dipole moment.Accordingly, the phosphate solvent can strongly interacts with an alkalimetal cation and can dissolve the alkali metal salt.

The substituents represented by R₁ to R₃ may be saturated aliphaticgroups. In such a case, all the atoms bonding to carbon atoms may behydrogen atoms or may be selected from hydrogen atoms and fluorineatoms.

In the electrolytic solution of Embodiment 1, the substituents R₁ to R₃may be trifluoroethyl groups.

The trifluoroethyl group is represented by CF₃—CH₂—.

Such a structure is excellent in electrochemical stability, in thestrength of interaction with an alkali metal cation, and in thecompatibility with a perfluoropolyether solvent.

As described above, the fluorine-containing solvent can contribute tothe charging and discharging reaction of an active material that canprovide a high voltage.

The fluorine-containing polar solvent can have improved affinity with aperfluoropolyether molecule. Consequently, the influence on energystabilization due to uniform compatibility can be enhanced.

In the electrolytic solution of Embodiment 1, the volume proportion ofthe perfluoropolyether to the nonaqueous solvent may be 10% or more and75% or less.

For example, the alkali metal salt of Embodiment 1 may be represented bya formula “MX”. The “M” of the alkali metal salt “MX” may be an alkalimetal. The “X” of the alkali metal salt “MX” may be Cl, Br, I, BF₄, PF₆,CF₃SO₃, ClO₄, CF₃CO₂, AsF₆, SbF₆, AlCl₄, N(CF₃SO₂)₂, N(FSO₂)₂,N(CF₃CF₂SO₂)₂, or N(CF₃SO₂)(FSO₂). The “X” of the alkali metal salt “MX”is preferably BF4, PF₆, ClO₄, N(CF₃SO₂)₂, or N(CF₃CF₂SO₂)₂ from theviewpoint of chemical stability, and is preferably N(CF₃SO₂)₂, N(FSO₂)₂,N(CF₃CF₂SO₂)₂, or N(CF₃SO₂)(FSO₂) from the viewpoint of solubility.These alkali metal salts may be used alone or as a mixture of two ormore thereof.

That is, the anion contained in the electrolytic solution of Embodiment1 may be at least one selected from the group consisting of BF₄ ⁻, PF₆⁻, N(SO₂CF₃)₂ ⁻, N(SO₂F)₂ ⁻, N(SO₂CF₂CF₃)₂ ⁻, N(SO₂—CF₂CF₂SO₂—)⁻, and[N—(SO₂F)—(SO₂CF₃)]⁻.

The composition described above can have improved solubility for analkali metal salt and also can provide an electrolytic solution having ahigh ionic conductivity.

In the electrolytic solution of Embodiment 1, the alkali metal cationmay be a lithium ion or a sodium ion.

Embodiment 2

Embodiment 2 will now be described, but the explanation duplicated withEmbodiment 1 is appropriately omitted.

The battery in Embodiment 2 includes the electrolytic solution ofEmbodiment 1, a positive electrode, and a negative electrode.

The positive electrode contains a positive electrode active materialthat has a property of occluding and releasing (i.e., can occlude andrelease) one or more alkali metal cations.

The negative electrode contains a negative electrode active materialthat has a property of occluding and releasing (i.e., can occlude andrelease) the one or more alkali metal cations.

Such a configuration can provide a battery achieving a high voltage andhaving a high energy density.

The battery of Embodiment 2 can be constituted, for example, as asecondary battery.

FIGURE is a schematic cross-sectional view illustrating an example ofthe battery according to Embodiment 2.

The battery shown in FIGURE includes a positive electrode 13, a negativeelectrode 16, a separator 17, and an outer package 18.

The positive electrode 13 is composed of a positive electrode collector11 and a positive electrode mixture layer 12 disposed on the positiveelectrode collector 11.

The negative electrode 16 is composed of a negative electrode collector14 and a negative electrode mixture layer 15 disposed on the negativeelectrode collector 14.

The positive electrode 13 and the negative electrode 16 face each otherwith the separator 17 therebetween.

The positive electrode 13, the negative electrode 16, and the separator17 are covered with the outer package 18 to form a battery.

The positive electrode mixture layer 12 may contain a positive electrodeactive material that can occlude and release alkali metal ions.

Examples of the positive electrode active material will now bedescribed.

When the alkali metal is lithium, the positive electrode active materialcan be a known material that can occlude and release lithium ions.Examples of the positive electrode active material include transitionmetal oxides and lithium-containing transition metal oxides, forexample, oxides of cobalt, oxides of nickel, oxides of manganese, oxidesof vanadium such as vanadium pentoxide (V₂O₅), and mixtures or complexoxides thereof; complex oxides containing lithium and transition metals,such as lithium cobaltate (LiCoO₂); and silicates of transition metalsand phosphates of transition metals such as lithium iron phosphate(LiFePO₄).

When the alkali metal is sodium, the positive electrode active materialcan be a known material that can occlude and release sodium ions.Examples of the positive electrode active material include transitionmetal oxides and sodium-containing transition metal oxides, for example,oxides of cobalt, oxides of nickel, oxides of manganese, oxides ofvanadium such as vanadium pentoxide (V₂O₅), and mixtures or complexoxides thereof; complex oxides containing sodium and transition metals,such as sodium manganate (NaMnO₂); and silicates of transition metalsand phosphates of transition metals.

The positive electrode collector 11 can be a porous or non-porous sheetor film made of a metal material, such as aluminum, stainless steel,titanium, or an alloy thereof. Aluminum and alloys thereof areinexpensive and can be readily formed into a thin film. The sheet orfilm can be, for example, metal foil or mesh. The surface of thepositive electrode collector 11 may be coated with a carbon material,such as carbon, for reducing the resistance value, providing a catalyticeffect, and enhancing the binding between the positive electrode mixturelayer 12 and the positive electrode collector 11.

The negative electrode mixture layer 15 may contain a negative electrodeactive material that can occlude and release alkali metal ions.

Examples of the negative electrode active material will now bedescribed.

When the alkali metal is lithium, the negative electrode active materialcan be a known material that can occlude and release lithium ions.Examples of the negative electrode active material include lithium metalelement, lithium metal alloys, carbon materials, and metal oxides.Examples of carbon material include graphite and non-graphite carbonmaterials, such as hard carbon and coke. Examples of the metal oxideinclude lithium titanate represented by Li₄Ti₅O₁₂. Examples of thelithium metal alloy include alloys of lithium with a silicon compound,tin compound, or aluminum compound.

When the alkali metal is sodium, the negative electrode active materialcan be a known material that can occlude and release sodium ions.Examples of the negative electrode active material include sodium metalelement, sodium metal alloys, carbon materials, and metal oxides.Examples of carbon material include graphite and non-graphite carbonmaterials, such as hard carbon and coke. Examples of the metal oxideinclude sodium titanate represented by Na₂Ti₃O₇. Examples of the sodiummetal alloy include alloys of sodium with a tin compound, germaniumcompound, zinc compound, bismuth compound, or indium compound.

The negative electrode collector 14 can be a porous or non-porous sheetor film made of a metal material, such as aluminum, stainless steel,nickel, copper, or an alloy thereof. Aluminum and alloys thereof areinexpensive and can be readily formed into a thin film. The sheet orfilm can be, for example, metal foil or mesh. The surface of thenegative electrode collector 14 may be coated with a carbon material,such as carbon, for reducing the resistance value, providing a catalyticeffect, and enhancing the binding between the negative electrode mixturelayer 15 and the negative electrode collector 14.

The positive electrode mixture layer 12 may contain a conductiveassistant, an ion conductor, a binder, or another component.

The negative electrode mixture layer 15 may contain a conductiveassistant, an ion conductor, a binder, or another component.

The conductive assistant can be used for reducing the electroderesistance. Examples of the conductive assistant include carbonmaterials, such as carbon black, graphite, and acetylene black; andconductive polymers, such as polyaniline, polypyrrole, andpolythiophene.

The ion conductor can be used for reducing the electrode resistance.Examples of the ion conductor include gel electrolytes, such aspolymethyl methacrylate; and solid electrolytes, such as polyethyleneoxide.

The binder is used for improving the binding properties of the materialconstituting the electrode. Examples of the binder includepolyvinylidene fluoride, vinylidene fluoride-hexafluoropropylenecopolymers, vinylidene fluoride-tetrafluoroethylene copolymers,polytetrafluoroethylene, carboxymethyl cellulose, polyacrylic acid,styrene-butadiene copolymer rubber, polypropylene, polyethylene, andpolyimide.

The separator 17 can be a porous film made of, for example,polyethylene, polypropylene, glass, cellulose, or ceramic. The porousfilm can be used by filling the pores with an electrolyte.

EXAMPLES

Examples and Comparative Examples will describe nonaqueous electrolyticsolutions as an aspect of the present disclosure, nonaqueous electrolytesecondary batteries produced using the nonaqueous electrolyticsolutions, and the results thereof.

The nonaqueous electrolytic solutions in Examples were all prepared inan argon glove box.

The composition of the present disclosure is not limited to thefollowing Examples.

Example 1

Nonaqueous electrolytic solutions were prepared using the followingperfluoropolyether, fluorinated phosphate solvent, and alkali metalsalt.

That is, the perfluoropolyether used was a perfluoropolyether(manufactured by Solvay Specialty Polymers, Galden HT-80) having aweight-average molecular weight of 430.

The fluorinated phosphate solvent used was a compound (TFEP) representedby Formula (1):

where the substituents R₁ to R₃ are trifluoroethyl (CF₃—CH₂—) groups.

The alkali metal salt used was lithium bis(fluorosulfonyl)imide(LiN(FSO₂)₂).

The perfluoropolyether was mixed with the fluorinated phosphate (TFEP)at a volume proportion of the perfluoropolyether to the total volume(total volume of the solvents) of 10%.

Subsequently, the alkali metal salt was dissolved in the solvent mixtureat a concentration of 0.36 M.

Nonaqueous electrolytic solution sample 1 was thus prepared.

Example 2

The same perfluoropolyether as that in Example 1 was mixed with the samefluorinated phosphate as that in Example 1 at a volume proportion of theperfluoropolyether to the total volume (total volume of the solvents) of25%.

Nonaqueous electrolytic solution sample 2 was prepared as in Example 1except the above.

Example 3

The same perfluoropolyether as that in Example 1 was mixed with the samefluorinated phosphate as that in Example 1 at a volume proportion of theperfluoropolyether to the total volume (total volume of the solvents) of50%.

Nonaqueous electrolytic solution sample 3 was prepared as in Example 1except the above.

Example 4

The same perfluoropolyether as that in Example 1 was mixed with the samefluorinated phosphate as that in Example 1 at a volume proportion of theperfluoropolyether to the total volume (total volume of the solvents) of75%.

Nonaqueous electrolytic solution sample 4 was prepared as in Example 1except the above.

Example 5

The solvent used was a perfluoropolyether (manufactured by SolvaySpecialty Polymers, Galden HT-170) having a weight-average molecularweight of 760.

Nonaqueous electrolytic solution sample 5 was prepared as in Example 1except the above.

Example 6

The solvent used was a perfluoropolyether (manufactured by SolvaySpecialty Polymers, Galden HT-230) having a weight-average molecularweight of 1020.

Nonaqueous electrolytic solution sample 6 was prepared as in Example 1except the above.

Comparative Example 1

Triethylene glycol dimethyl ether (CH₃—(OCH₂CH₂)₃—OCH₃) was used insteadof the fluorinated phosphate in Example 1.

Nonaqueous electrolytic solution sample 7 was prepared as in Example 1except the above.

Comparative Example 2

The same perfluoropolyether as that in Comparative Example 1 was mixedwith the same triethylene glycol dimethyl ether as that in ComparativeExample 1 at a volume proportion of the perfluoropolyether to the totalvolume (total volume of the solvents) of 25%.

Nonaqueous electrolytic solution sample 8 was prepared as in ComparativeExample 1 except the above.

Comparative Example 3

Monoethylene glycol dimethyl ether (CH₃—(OCH₂CH₂)₁—OCH₃) was usedinstead of the fluorinated phosphate in Example 1.

Nonaqueous electrolytic solution sample 9 was prepared as in Example 1except the above.

Comparative Example 4

The same perfluoropolyether as that in Comparative Example 3 was mixedwith the same monoethylene glycol dimethyl ether as that in ComparativeExample 3 at a volume proportion of the perfluoropolyether to the totalvolume (total volume of the solvents) of 25%.

Nonaqueous electrolytic solution sample 10 was prepared as inComparative Example 3 except the above.

Comparative Example 5

Triethyl phosphate was used instead of the fluorinated phosphate inExample 1.

Nonaqueous electrolytic solution sample 11 was prepared as in Example 1except the above.

Comparative Example 6

The same perfluoropolyether as that in Comparative Example 5 was mixedwith the same triethyl phosphate as that in Comparative Example 5 at avolume proportion of the perfluoropolyether to the total volume (totalvolume of the solvents) of 25%.

Nonaqueous electrolytic solution sample 12 was prepared as inComparative Example 5 except the above.

[Evaluation of Compatibility and Conductivity]

The nonaqueous electrolytic solutions of Examples 1 to 6 and ComparativeExamples 1 to 6 were visually evaluated for compatibility. Thenonaqueous solvents judged to be uniform were measured for theconductivity. The conductivity was measured at 60° C.

Table 1 shows the results of evaluation of the compatibility and theconductivity of the nonaqueous electrolytic solutions of Examples 1 to 6and Comparative Examples 1 to 6.

TABLE 1 Weight-average Second component Volume proportion of Evaluationmolecular weight of other than perfluoropolyether results ofConductivity perfluoropolyether perfluoropolyether [%] compatibility[10⁻⁶ S/cm] Example 1 430 Fluorinated 10 ◯ 814 Example 2 phosphate 25 ◯510 Example 3 50 ◯ 140 Example 4 75 ◯ 8.84 Example 5 760 10 ◯ 772Example 6 1020 10 ◯ 698 Comparative 430 Triethylene glycol 10 X —Example 1 dimethyl ether Comparative 25 X — Example 2 ComparativeMonoethylene glycol 10 X — Example 3 dimethyl ether Comparative 25 X —Example 4 Comparative Triethyl phosphate 10 X — Example 5 Comparative 25X — Example 6

In Table 1, “compatibility: x” means that deposition of the alkali metalsalt or phase separation of the solvents was observed.

In Table 1, “compatibility: ◯” means that no deposition of the alkalimetal salt or no phase separation of the solvents was observed.

As shown in Table 1, the nonaqueous electrolytic solutions of Examples 1to 6 were prepared as uniform electrolytic solvents that did not causephase separation even in the case of containing a volume proportion of10% or more of the perfluoropolyether.

In particular, the nonaqueous electrolytic solutions of Examples 1 to 4each containing a perfluoropolyether having a molecular weight of 430and a fluorinated phosphate were uniformly mixed in a broad compositionrange, i.e., in a volume proportion of the perfluoropolyether solvent of10% to 75%.

In contrast, nonaqueous electrolytic solution samples 7 to 12 ofComparative Examples 1 to 6 containing nonaqueous solvents that areusually used as the nonaqueous electrolytes for lithium secondarybatteries instead of the fluorinated phosphate were not uniform, andphase separation was observed.

It was accordingly demonstrated that the fluorinated phosphate works fordissolving an alkali metal salt and for preparing a uniform solution.

The phosphate ester group of triethyl phosphate used in ComparativeExamples 5 and 6 is ethyl group and differs from the trifluoroethylgroup used in Examples 1 to 6 in whether fluorine is contained or not.The electrolytic solutions of Examples 1 to 6 were uniformly compatible,whereas the electrolytic solutions of Comparative Examples 5 and 6caused phase separation. This demonstrated that an unsubstitutedphosphate is insufficient for preparing a uniform solution, and afluorinated phosphate is effective.

Example 7

Example 7 relates to a lithium secondary battery containing a nonaqueouselectrolytic solution.

The positive electrode active material was LiNiCoAlO₂.

The positive electrode active material, acetylene black as a conductiveassistant, and polyvinylidene fluoride as a binder were weighed at aweight ratio of 8:1:1, and the mixture was dispersed in an NMP solventto prepare a slurry.

The resulting slurry was applied to an Al collector with a coater.

The electrode plate coated with the slurry was rolled with a rollingmill, was punched into a 20 mm square, and was processed into anelectrode state to prepare a positive electrode.

A negative electrode was produced by pressure-bonding lithium metal to a20 mm square nickel mesh.

The positive electrode and the negative electrode were disposed so as toface each other with a polyethylene microporous film as the separatortherebetween to produce an electrode group having a configurationdescribed in Embodiment 2.

Nonaqueous electrolytic solution sample 3 of Example 3 was used as theelectrolytic solution.

The electrolytic solution was poured to the electrode group, and sealingwas performed to produce a laminated lithium secondary battery.

[Charging and Discharging Test]

The lithium secondary battery of Example 7 was subjected to a chargingand discharging test under the following conditions.

The charging and discharging test was performed in a thermostaticchamber of 60° C.

In the test, charging was first performed, and the battery was pausedfor 30 minutes, followed by discharging. This charging and dischargingwere repeated three times.

The charging was performed at a constant current and a constant voltagewith a current of 0.05 C rate with respect to the theoretical capacityof the positive electrode active material. The upper limit chargingvoltage was 4.2 V. The lower limit current value at the constant voltagewas 0.02 C rate.

The discharging was performed at a lower limit discharging voltage of2.5 V and a current of 0.05 C rate. After pausing for 30 minutes,discharging was performed at a current of 0.02 C rate.

The charging and discharging operation was repeated three times. On thisoccasion, stable charging and discharging operation was confirmed. Afterthe confirmation, the discharging capacity on the third dischargingoperation was converted into the capacity per 1 g of each positiveelectrode active material (mAhg⁻¹).

Table 2 shows the resulting discharging capacities.

TABLE 2 Solvent composition Volume proportion of Discharge Solvent otherthan perfluoropolyether capacity perfluoropolyether [%] [mAhg⁻¹] Example7 Fluorinated phosphate 50 210 (TFEP)

The electrolytic solutions of Comparative Examples 1 to 6 caused phaseseparation and could not be subjected to the charging and dischargingtest.

In contrast, as shown in Table 2, the battery of Example 7 had adischarging capacity of 210 mAhg⁻¹.

The results demonstrated that the electrolytic solution of Example 7 hadsufficient electrochemical stability capable of withstanding chargingand discharging operation of the battery, in spite of a large amount (avolume proportion of 50%) of the perfluoropolyether, which is a flameretardant, contained in the electrolytic solutions.

The electrolytic solution of the present disclosure can be used as theelectrolytic solution of a battery.

What is claimed is:
 1. An electrolytic solution comprising: a nonaqueoussolvent; and an alkali metal salt, wherein the alkali metal salt isdissolved in the nonaqueous solvent; and the nonaqueous solvent containsa perfluoropolyether and a fluorinated phosphate, wherein theperfluoropolyether is CF₃—O—(CF₂—CF(CF₃)—O)_(p)—(CF₂—O)_(q)—CF₃ orCF₃—O—(C₃F₆—O)_(p)—(CF₂—O)_(q)—CF₃, wherein p and q are selected so thatthe perfluoropolyether has a weight average molecular weight of about350 to less than
 1100. 2. The electrolytic solution according to claim1, wherein the fluorinated phosphate contains a compound represented byFormula (1):

where, R₁ to R₃ each independently represent an aromatic group, anunsaturated aliphatic group, or a saturated aliphatic group, wherein thearomatic group, the unsaturated aliphatic group, and the saturatedaliphatic group has at least one fluorine atom substituted for thehydrogen atom and contains a halogen atom, a nitrogen atom, an oxygenatom, a sulfur atom, or a silicon atom; and the unsaturated aliphaticgroup and the saturated aliphatic group are straight chains or arecyclic.
 3. The electrolytic solution according to claim 2, wherein R₁ toR₃ represent trifluoroethyl groups.
 4. The electrolytic solutionaccording to claim 1, wherein the nonaqueous solvent contains theperfluoropolyether at a volume proportion of the perfluoropolyether tothe nonaqueous solvent of 10% or more and 75% or less.
 5. Theelectrolytic solution according to claim 1, wherein the alkali metalsalt is composed of an alkali metal cation and an anion; and the anionis at least one selected from the group consisting of BF₄ ⁻, PF₆ ⁻,N(SO₂CF₃)₂ ⁻, N(SO₂F)₂ ⁻, N(SO₂CF₂CF₃)₂ ⁻, N(SO₂—CF₂CF₂SO₂—)⁻, and[N—(SO₂F)—(SO₂CF₃)]⁻.
 6. The electrolytic solution according to claim 1,wherein the alkali metal salt is composed of an alkali metal cation andan anion; and the alkali metal cation is a lithium ion or a sodium ion.7. A battery comprising: an electrolytic solution; a positive electrodecontaining a positive electrode active material that has a property ofoccluding and releasing an alkali metal cation; and a negative electrodecontaining a negative electrode active material that has a property ofoccluding and releasing the alkali metal cation, wherein theelectrolytic solution contains a nonaqueous solvent and an alkali metalsalt; the alkali metal salt is composed of the alkali metal cation andan anion; the alkali metal salt is dissolved in the nonaqueous solvent;and the nonaqueous solvent contains a perfluoropolyether and afluorinated phosphate, wherein the perfluoropolyether isCF₃—O—(CF₂—CF(CF₃)—O)_(p)—(CF₂—O)_(q)—CF₃ orCF₃—O—(C₃F₆—O)_(p)—(CF₂—O)_(q)—CF₃, wherein p and q are selected so thatthe perfluoropolyether has a weight average molecular weight of about350 to less than 1100.